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Webrep - Cgi 4

This final report from Infinity Diagnostics Laboratories summarizes the results of a COVID-19 PCR test performed on a sample collected from Viridiana Bonilla. The test returned a negative result for SARS-CoV-2. Some limitations of the RT-PCR test used are noted, including that negative results do not rule out infection and that improper specimen handling could impact the test's performance. The report was reviewed and signed by the laboratory director, Dr. Farhad Setoodah.

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59 views1 page

Webrep - Cgi 4

This final report from Infinity Diagnostics Laboratories summarizes the results of a COVID-19 PCR test performed on a sample collected from Viridiana Bonilla. The test returned a negative result for SARS-CoV-2. Some limitations of the RT-PCR test used are noted, including that negative results do not rule out infection and that improper specimen handling could impact the test's performance. The report was reviewed and signed by the laboratory director, Dr. Farhad Setoodah.

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viridiana bonilla
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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FINAL REPORT

INFINITY DIAGNOSTICS LABORATORIES


370 NORTH STREET
TETERBORO, NJ 07608-1209
(973)528-8070 Fax: (201)365-6068
CHAI URGENT CARE BONILLA, VIRIDIANA Accession #: 2111111105
400 NEW HAMPSHIRE AVE DOB: 05/13/1980 Age: 41 Specimen ID:
LAKEWOOD, NJ 08701 Sex: F Date Collected:11/10/21 14:49
Acct: 9136 ID#: 425904 Date Received: 11/11/21 02:34
Phone: (732) 994-2423 Address: 516 5Th Street
Jackson, NJ 08527 Date of Report:11/11/21
Phys: SCHWARTZMAN, EYAL M.D. Phone: (732) 804-4137 First Reported:11/11/21

CLINICAL REPORT
Comments:

Fasting: NONFASTING

COVID-19 PCR
Test Result Abnormal Reference Units Previous Result Date
SARS-Cov-2 RT-PCR NEGATIVE NEGATIVE

SOURCE :NASOPHARYNGEAL.
LIMITATIONS:
-Applied BioSystems,iAMP COVID-19 Detection Kit is a real-time fluorscent
reverse transcription isothermal assay RT-PCR TEST.
-This test is a qualitative in vitro diagnostic test that has been
authorized by FDA under an EUA for use by authorized Laboratories.
-This test is RT-PCR utilized in detection of nucleic acid from the
SARS-Cov-2 RNA in nasopharyngeal swab specimens collected during
the acute phase of infection.
-Negative results do not preclude infection with SARS-COV-2 virus and
should not be the sole basis of a patient management decision.
-Improper collection, transport, or storage of specimens may impact the
ability of the assay to perform as indicated.
-The impacts of vaccines, antiviral therapeutic, antibiotics,
chemotherapeutic, or immuno-suppressant drugs have not been evaluated.

________________________________ END OF REPORT __________________________

Laboratory Director: Farhad Setoodah M.D.


Page 1
370 NORTH STREET | TETERBORO, NJ 07608-1209 | (973)528-8070 Printed 11/11/21 15:02

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